Literature DB >> 29380664

Wernicke-Korsakoff syndrome as a rare phenotype of sporadic Creutzfeldt-Jakob disease.

Joanna Bielewicz1, Anna Szczepańska-Szerej1, Magdalena Ogórek1, Piotr Dropko1, Katarzyna Wojtal2, Konrad Rejdak1.   

Abstract

We reported the case of a patient with Wernicke-Korsakoff syndrome (WKs) as an early clinical manifestation of sporadic Creutzfeld-Jakob disease (sCJD). The 66-year-old female complained of dizziness and imbalance which mostly occurred while walking. A neurological examination revealed a triad of symptoms characteristic for WKs such as gaze paresis, ataxia of limbs and trunk as well as memory disturbances with confabulations. The disturbances increased during the course of the disease, which led to the death of the patient four months after the appearance of the signs. The patient was finally diagnosed with sCJD disease. The most useful ancillary examination results supporting sCJD diagnosis were brain diffusion DWI MRI (diffusion weighted magnetic resonance imaging) and the presence of 14-3-3 protein in CSF (cerebrospinal fluid). Since that manifestation of sCJD is very unique other causes should be taken into consideration while making a final diagnosis.

Entities:  

Keywords:  DWI MRI; Wernicke-Korsakoff syndrome; dementia; prion diseases; sporadic Creutzfeld-Jakob disease

Mesh:

Substances:

Year:  2018        PMID: 29380664      PMCID: PMC6016515          DOI: 10.1080/19336896.2018.1433988

Source DB:  PubMed          Journal:  Prion        ISSN: 1933-6896            Impact factor:   3.931


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